Linked Data
MyVariant Identifiers:
chr6:g.18122418A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18122187A>G , CM000668.2:g.18122187A>G | GRCh38 |
| NC_000006.11:g.18122418A>G , CM000668.1:g.18122418A>G | GRCh37 |
| NC_000006.10:g.18230397A>G | NCBI36 |
| NG_016750.1:g.5434T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000340650.6:c.420T>C MANE Select | ENSP00000345464.3:p.Arg140= | |
| ENST00000340650.4:c.420T>C | ENSP00000345464.3:p.Arg140= | |
| NM_198586.2:c.420T>C | NP_940988.2:p.Arg140= | |
| NM_198586.3:c.420T>C MANE Select | NP_940988.2:p.Arg140= |